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R Barnes

Publications and source records attributed to R Barnes.

At least 181 records · Page 10Linked to original sources

Temperature of compensation: significance for virus in- activation.

The purpose of this report is to call attention to the probable biological utility of a physical constant, the temperature of compensation (T(c)) or isokinetic temperature. T(c) has hitherto not been used in biological research. It is defined as the temperature at which a series of Arrhenius plots, related by variation of a single parameter, pass through a common point. Such systems demonstrate the so-called compensation effect and show linear variation of change in enthalpy with change in entropy; the slope [unk] H/[unk]S is T(c). Related reactions in which, for example, solvent change or structural change of the reactants does not change the mechanism of the reaction or the nature of the transition state exhibit an identical T(c). The system used in this study was a complex one, i.e., protection against thermal inactivation of Sindbis virus by HPO(4) (=) and SO(4) (=). The time-rate constant of loss of infectivity was determined at different temperatures for virus suspended in different salt concentrations at constant pH. The compensation effect was demonstrated and T(c) was found to be approximately 57 degrees C for virus inactivation in both Na(2)HPO(4) and MgSO(4) solutions. The intercept of a DeltaSdouble dagger/DeltaHdouble dagger plot, defined as the constant B, also was the same for the two salts. We suggest that determination of T(c) in biological systems might be of value in (1) establishment of whether an observed phenomenon results from the same process or mechanism as another observed phenomenon; (2) prediction of rates or other behavior under relevant conditions; and (3) classification.

Arboviruses↗

Automated instrument for the fluorescent treponemal antibody-absorption test and other immunofluorescence tests.

An automated diagnostic test instrument and its development program are described. The instrument automates the fluorescent treponemal antibody-absorption test for syphilis to the extent that only 4 hr of technician time is required to conduct approximately 200 tests daily. Evaluation to date suggests its efficacy. In addition, preliminary studies indicate the feasibility of detecting antibodies to Toxoplasma gondii, Plasmodium malariae, and nucleoprotein (antinuclear factor). The instrument would seem to have broad application for routine and research immunofluorescence testing. Two elements comprise the instrument: a slide processor and a microscope attachment. The slide processor is an electro-pneumatically actuated device which automatically feeds special laboratory slides, on which antigen or other reagents are prefixed, through a series of operations which provide reagent application, incubation, washing, drying, and stacking of the finished slides for readout. The instrument provides flexibility in that incubation time and temperature as well as point, sequence, and duration of reagent application can be varied to accommodate a variety of immunofluorescence techniques. The microscope attachment can be fitted to all conventional dark-field fluorescence microscopes and makes possible the reading of three to six slides per minute. The reacted slides from the processor are injected sequentially onto the stage of the microscope by movement of a lever. As injected, slides are automatically in visual focus; fine focus is occasionally required. Scanning of the reacted field is accomplished by means of the normal microscope controls. A buffered glycerol coupling is maintained between the darkfield condenser substage lens and the slide cover glass by means of a pushbutton-actuated feed system.

Absorption↗

Mercurialism.

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Adult↗